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Kallmann Syndrome
A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and olfactory nerve defects. It is characterized by congenital HYPOGONADOTROPIC hypogonadism and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (genetic diseases, x-linked), an autosomal dominant, or an autosomal recessive trait.
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 Kallmann syndrome - Wikipedia en.wikipedia.org |  and Kallmann's syndrome kallmanns.org |  In Kallmann syndrome, the www.devbio.com |  of Kallmann's Syndrome library.med.utah.edu |
 both Kallmann syndrome and www.pnas.org |  Kallmann syndrome www.nature.com |  In Kallmann's syndrome, it is kallmanns.org |  page for Kallmann syndrome www.textmed.com |
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Wikipedia
Kallmann McKinnell & Wood, Kallmann syndrome, Anosmin-1, Hartmut Kallmann, KAL1 gene, Gerhard Kallmann, Franz Josef Kallmann, Kal?m cosmological argument, KAL (UK), Oru Kal Oru Kannadi
More information
- Reported cases - Summary of cases reported on this disease.
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